Peterson K, Walker R W
Department of Neurology, Memorial Sloan-Kettering Cancer Center, New York, NY.
Neurology. 1995 Mar;45(3 Pt 1):440-2. doi: 10.1212/wnl.45.3.440.
Medulloblastoma/primitive neuroectodermal tumor (PNET) is an uncommon tumor in adults. We reviewed the medical records of 45 patients, 15 years or older, with medulloblastoma/PNET. Most patients presented with symptoms referable to the posterior fossa, and 31 of 45 patients had disease limited to the posterior fossa at the time of diagnosis. Despite initial favorable response to surgical resection, radiation, and chemotherapy, one-half had recurrence 10 to 76 months after initial treatment. Only two of these patients had local recurrence; the remainder had CNS dissemination, systemic metastasis, or both. The recommended approach to medulloblastoma/PNET in adults is similar to that in children, and includes initial staging evaluation, systemic and focal therapy (ie, neuraxis irradiation with posterior fossa boost and chemotherapy), and long-term follow-up to detect late and distant recurrence.
髓母细胞瘤/原始神经外胚层肿瘤(PNET)在成人中是一种罕见肿瘤。我们回顾了45例年龄在15岁及以上的髓母细胞瘤/PNET患者的病历。大多数患者表现出与后颅窝相关的症状,45例患者中有31例在诊断时疾病局限于后颅窝。尽管对手术切除、放疗和化疗最初反应良好,但一半患者在初始治疗后10至76个月出现复发。这些患者中只有2例有局部复发;其余患者有中枢神经系统播散、全身转移或两者皆有。成人髓母细胞瘤/PNET的推荐治疗方法与儿童相似,包括初始分期评估、全身和局部治疗(即后颅窝加量的全脑脊髓照射和化疗),以及长期随访以检测晚期和远处复发。